| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 118651 | BAA10g11090 | A10 | 12778058 | G | A | upstream_gene_variant | MODIFIER | c.-4218C>T| |
S202 |
| 118652 | BAA10g11090 | A10 | 12778780 | C | T | upstream_gene_variant | MODIFIER | c.-4940G>A| |
S166 |
| 118653 | BAA10g11110 | A10 | 12779300 | C | T | upstream_gene_variant | MODIFIER | c.-4426C>T| |
S183 |
| 118654 | BAA10g11110 | A10 | 12783364 | G | A | upstream_gene_variant | MODIFIER | c.-362G>A| |
S291 |
| 118655 | BAA10g11110 | A10 | 12784266 | G | A | missense_variant | MODERATE | c.541G>A|p.Gly181Arg |
S302 |
| 118656 | BAA10g11110 | A10 | 12784874 | G | A | downstream_gene_variant | MODIFIER | c.*184G>A| |
S240 |
| 118657 | BAA10g11110 | A10 | 12785178 | C | T | downstream_gene_variant | MODIFIER | c.*488C>T| |
S51 |
| 118658 | BAA10g11110 | A10 | 12785231 | C | T | downstream_gene_variant | MODIFIER | c.*541C>T| |
S114 |
| 118659 | BAA10g11110 | A10 | 12785677 | C | T | downstream_gene_variant | MODIFIER | c.*987C>T| |
S168 |
| 118660 | BAA10g11130 | A10 | 12785999 | G | C | upstream_gene_variant | MODIFIER | c.-4827G>C| |
|
| 118661 | BAA10g11130 | A10 | 12786007 | G | A | upstream_gene_variant | MODIFIER | c.-4819G>A| |
S18 |
| 118662 | BAA10g11130 | A10 | 12786058 | C | T | upstream_gene_variant | MODIFIER | c.-4768C>T| |
S199 |
| 118663 | BAA10g11130 | A10 | 12786177 | G | A | upstream_gene_variant | MODIFIER | c.-4649G>A| |
S176 |
| 118664 | BAA10g11130 | A10 | 12786325 | G | A | upstream_gene_variant | MODIFIER | c.-4501G>A| |
S219 S72 |
| 118665 | BAA10g11130 | A10 | 12786590 | G | A | upstream_gene_variant | MODIFIER | c.-4236G>A| |
S71 |
| 118666 | BAA10g11120 | A10 | 12789149 | C | T | upstream_gene_variant | MODIFIER | c.-813G>A| |
S180 |
| 118667 | BAA10g11120 | A10 | 12789241 | C | T | upstream_gene_variant | MODIFIER | c.-905G>A| |
S133 |
| 118668 | BAA10g11130 | A10 | 12790845 | G | A | missense_variant | MODERATE | c.20G>A|p.Gly7Asp |
S296 |
| 118669 | BAA10g11130 | A10 | 12790977 | C | T | missense_variant | MODERATE | c.152C>T|p.Pro51Leu |
S287 |
| 118670 | BAA10g11130 | A10 | 12791920 | G | A | missense_variant | MODERATE | c.895G>A|p.Asp299Asn |
S100 |
| 118671 | BAA10g11130 | A10 | 12792079 | C | T | synonymous_variant | LOW | c.1054C>T|p.Leu352Leu |
S252 |
| 118672 | BAA10g11120 | A10 | 12792165 | G | A | upstream_gene_variant | MODIFIER | c.-3829C>T| |
S11 |
| 118673 | BAA10g11130 | A10 | 12794258 | G | A | downstream_gene_variant | MODIFIER | c.*2159G>A| |
S136 |
| 118674 | BAA10g11130 | A10 | 12794322 | C | T | downstream_gene_variant | MODIFIER | c.*2223C>T| |
S46 |
| 118675 | BAA10g11130 | A10 | 12795783 | C | T | downstream_gene_variant | MODIFIER | c.*3684C>T| |
S191 |